Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H12 |
Molecular Weight | 84.1595 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)C=C
InChI
InChIKey=PKXHXOTZMFCXSH-UHFFFAOYSA-N
InChI=1S/C6H12/c1-5-6(2,3)4/h5H,1H2,2-4H3
Molecular Formula | C6H12 |
Molecular Weight | 84.1595 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Copper(I)-homoscorpionate catalysts for the preferential, kinetically controlled cis cyclopropanation of alpha-olefins with ethyl diazoacetate. | 2002 Feb 13 |
|
Re-based heterogeneous catalysts for olefin metathesis prepared by surface organometallic chemistry: reactivity and selectivity. | 2003 Feb 17 |
|
Vibrational spectra and ab initio analysis of tert-butyl, trimethylsilyl, and trimethylgermyl derivatives of 3,3-dimethylcyclopropene. I. 3,3-Dimethyl-1,2-bis(tert-butyl)cyclopropene. | 2003 Jan 15 |
|
Vibrational spectra and ab initio analysis of tert-butyl, trimethylsilyl, and trimethylgermyl derivatives of 3,3-dimethylcyclopropene III. 3,3-Dimethyl-1-(trimethylsilyl)cyclopropene. | 2003 Jul |
|
Mechanism of alkane transfer-dehydrogenation catalyzed by a pincer-ligated iridium complex. | 2003 Jul 2 |
|
Vibrational spectra and ab initio analysis of tert-butyl, trimethylsilyl, and trimethylgermyl derivatives of 3,3-dimethylcyclopropene IV. 3,3-dimethyl-1,2-bis(trimethylgermyl)cyclopropene. | 2003 Jun |
|
The Rh4(CO)12-catalyzed hydroformylation of 3,3-dimethylbut-1-ene promoted with HMn(CO)5. Bimetallic catalytic binuclear elimination as an origin for synergism in homogeneous catalysis. | 2003 May 7 |
|
Vibrational spectra and ab initio analysis of tert-butyl, trimethylsilyl, and trimethylgermyl derivatives of 3,3-dimethyl cyclopropene V. 3,3-dimethyl-1-(trimethylgermyl)cyclopropene. | 2004 Feb |
|
Oxidative C-arylation of free (NH)-heterocycles via direct (sp3) C-H bond functionalization. | 2004 Oct 20 |
|
A practical, fast, and high-yielding aziridination procedure using simple Cu(II) complexes containing N-donor pyridine-based ligands. | 2005 Jun 10 |
|
Cationic rhodium mono-phosphine fragments partnered with carborane monoanions [closo-CB11H6X6]- (X = H, Br). Synthesis, structures and reactivity with alkenes. | 2007 Nov 14 |
|
Intramolecular alkyl phosphine dehydrogenation in cationic rhodium complexes of tris(cyclopentylphosphine). | 2008 |
|
Sunflower-based feedstocks in nonfood applications: Perspectives from olefin metathesis. | 2008 Aug |
|
Iridium derivatives of fluorinated aromatics by C-H activation: isolation of classical and non-classical hydrides. | 2008 Oct 14 |
|
Homogeneous catalytic transfer dehydrogenation of alkanes with a group 10 metal center. | 2009 Nov 7 |
|
Vibrational spectra and ab initio analysis of tert-butyl, trimethylsilyl, trimethylgermyl, trimethylstannyl and trimethylplumbyl derivatives of 3,3-dimethylcyclopropene. XII. 1,2-Di-tert-butyl-3,3-dimethylcyclopropene. | 2010 Apr |
|
Concurrent synergism and inhibition in bimetallic catalysis: catalytic binuclear elimination, solute-solute interactions and a hetero-bimetallic hydrogen-bonded complex in rh-mo hydroformylations. | 2010 Apr 7 |
|
Dehydrogenation of saturated CC and BN bonds at cationic N-heterocyclic carbene stabilized M(III) centers (M = Rh, Ir). | 2010 Aug 4 |
|
C-H bond activation/borylation of furans and thiophenes catalyzed by a half-sandwich iron N-heterocyclic carbene complex. | 2010 Jul 5 |
|
Copolymerization of ethylene with sterically hindered 3,3-dimethyl-1-butene using a chain-walking pd-diimine catalyst. | 2010 Jun 16 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:44:24 GMT 2023
by
admin
on
Fri Dec 15 19:44:24 GMT 2023
|
Record UNII |
01ZB73D2KK
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID1027211
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY | |||
|
01ZB73D2KK
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY | |||
|
558-37-2
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY | |||
|
Neohexene
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY | |||
|
209-195-9
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY | |||
|
11210
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY | |||
|
74119
Created by
admin on Fri Dec 15 19:44:24 GMT 2023 , Edited by admin on Fri Dec 15 19:44:24 GMT 2023
|
PRIMARY |